Medical Device Manufacturer · US , San Mateo , CA

Osteotech, Inc. - FDA 510(k) Cleared Devices

24 submissions · 21 cleared · Since 1985
24
Total
21
Cleared
0
Denied

Osteotech, Inc. has 21 FDA 510(k) cleared orthopedic devices. Based in San Mateo, US.

Historical record: 21 cleared submissions from 1985 to 2008.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

24 devices
1–12 of 24
GRAFTON R II EDBM, DEMINERALIZED BONE MATRIX ALLOGRAFT, RESORBABLE CALCIUM SALT BONE VOID FILLER DEVICES
K082615 · MQV Filler, Bone Void, Calcium Compound · Orthopedic
Oct 2008 37d
PLEXUR M
K081227 · MQV Filler, Bone Void, Calcium Compound · Orthopedic
Jul 2008 83d
PLEXUR-P
K080511 · MQV Filler, Bone Void, Calcium Compound · Orthopedic
Apr 2008 56d
PLEXUR M
K073405 · MQV Filler, Bone Void, Calcium Compound · Orthopedic
Mar 2008 90d
PLEXUR P
K061982 · MBP Filler, Bone Void, Osteoinduction (w/o Human Growth Factor) · Orthopedic
Feb 2007 209d
GRAFTON DBM
K051188 · NUN Bone Grafting Material, Human Source · Dental
Jan 2006 238d
GRAFTON DBM
K051195 · MBP Filler, Bone Void, Osteoinduction (w/o Human Growth Factor) · Orthopedic
Dec 2005 220d
GRAFTCAGE TLX
K051781 · MQP Spinal Vertebral Body Replacement Device · Orthopedic
Dec 2005 168d
VIAGRAF DBM PASTE
K043209 · MBP Filler, Bone Void, Osteoinduction (w/o Human Growth Factor) · Orthopedic
Dec 2005 381d
GRAFTCAGE ACX
K053080 · MQP Spinal Vertebral Body Replacement Device · Orthopedic
Dec 2005 29d
GRAFTON PLUS DBM PASTE
K042707 · NUN Bone Grafting Material, Human Source · Dental
Nov 2005 426d
GRAFTON PLUS DBM PASTE
K043048 · MBP Filler, Bone Void, Osteoinduction (w/o Human Growth Factor) · Orthopedic
Nov 2005 384d
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